Preferred Name

Reye syndrome

ID

http://www.orpha.net/ORDO/Orphanet_3096

definition

A rare, systemic disease characterized by persistent vomiting with confusion, lethargy, disorientation, hyperreflexia, hyperventilation, and tachycardia, with rapid progression to seizures, non-inflammatory encephalopathy, coma and death. It typically develops between 12 hours and 3 weeks after recovery from a viral illness, such as upper respiratory tract infection or gastroenteritis. Hepatomegaly, acute hepatic steatosis, fatty liver degeneration and multiple laboratory abnormalities are associated.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3096

hasDbXref

ICD-10:G93.7

ICD-11:8E46

MeSH:D012202

MedDRA:10039012

UMLS:C0035400

label

Reye syndrome

notation

ORPHA:3096

part_of

http://www.orpha.net/ORDO/Orphanet_182222

prefixIRI

ORDO:Orphanet_3096

prefLabel

Reye syndrome

treeView

http://www.orpha.net/ORDO/Orphanet_182222

subClassOf

http://www.orpha.net/ORDO/Orphanet_377788

http://www.orpha.net/ORDO/Orphanet_557493

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